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老年正常人晶状体中谷胱甘肽扩散的障碍:核性白内障的一个可能先决条件。

An impediment to glutathione diffusion in older normal human lenses: a possible precondition for nuclear cataract.

作者信息

Sweeney M H, Truscott R J

机构信息

Australian Cataract Research Foundation, University of Wollongong, N. S.W., 2522, Australia.

出版信息

Exp Eye Res. 1998 Nov;67(5):587-95. doi: 10.1006/exer.1998.0549.

Abstract

Human age-related nuclear cataract is associated with progressive and widespread oxidation of proteins, particularly in the centre of the lens. The reasons for the onset of cataract and why this disease should take place only in the lenses of older individuals remain unclear. However, a common feature of nuclear cataract is the low concentration of reduced glutathione (GSH) in the centre of the lens. GSH is the principal lenticular antioxidant of the lens and it is synthesized and regenerated in the lens cortex. In this study we investigated the diffusion of glutathione within the human lens as a function of age. Normal human lenses were incubated in artificial aqueous humor containing [35S]cysteine and the label was metabolically incorporated into GSH. After 48-h incubation, lenses were sectioned and phosphorimaging was used to determine the distribution of 35S label. In young lenses, label appeared to diffuse uniformly throughout the whole lens. By contrast, in lenses over the age of 30, very little 35S had penetrated to the centre of the lens. A distinct zonal pattern of label distribution was noted in the older lenses after 48 h incubation, which had dimensions of approximately 7.2 mm (diameter) by 2.8 mm (axial). In some older lenses this pattern was noticeable even after 96-h incubation. Thus a barrier to the diffusion of GSH was observed in older normal lenses which was not present in younger lenses. Furthermore, the internal zone thus delineated has dimensions that coincide with those of the coloured and sclerotic zone present in nuclear cataract lenses. Since nuclear cataract is a disease of the elderly, and maintenance of GSH is known to be vital for lens clarity, we propose that the development of a barrier to the movement of GSH from its site of synthesis and regeneration in the cortex, into the nucleus in older normal lenses, may over time allow oxidative modification of protein to take place in the nucleus, resulting ultimately in nuclear cataract.

摘要

人类年龄相关性核性白内障与蛋白质的进行性广泛氧化有关,尤其是在晶状体中央。白内障发病的原因以及为何这种疾病仅发生在老年人的晶状体中仍不清楚。然而,核性白内障的一个共同特征是晶状体中央还原型谷胱甘肽(GSH)浓度较低。GSH是晶状体主要的抗氧化剂,在晶状体皮质中合成和再生。在本研究中,我们研究了谷胱甘肽在人晶状体中的扩散与年龄的关系。将正常人晶状体置于含有[35S]半胱氨酸的人工房水中孵育,标记物经代谢掺入GSH。孵育48小时后,将晶状体切片,用磷光成像法测定35S标记物的分布。在年轻晶状体中,标记物似乎均匀地扩散到整个晶状体。相比之下,在30岁以上的晶状体中,很少有35S渗透到晶状体中央。孵育48小时后,在老年晶状体中观察到标记物分布呈明显的带状模式,其尺寸约为7.2毫米(直径)×2.8毫米(轴向)。在一些老年晶状体中,即使孵育96小时后这种模式仍很明显。因此,在老年正常晶状体中观察到了GSH扩散的屏障,而年轻晶状体中不存在这种屏障。此外,如此划定的内部区域的尺寸与核性白内障晶状体中出现的有色和硬化区域的尺寸一致。由于核性白内障是一种老年疾病,并且已知维持GSH对晶状体透明度至关重要,我们提出,在老年正常晶状体中,GSH从其在皮质中的合成和再生部位向核内移动的屏障的形成,可能随着时间的推移使核内蛋白质发生氧化修饰,最终导致核性白内障。

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